Showing 15,541 - 15,560 results of 103,558 for search '(( 2 step decrease ) OR ( 5 ((point decrease) OR (((mean decrease) OR (a decrease)))) ))', query time: 1.51s Refine Results
  1. 15541

    Peroxovanadate Imidazole Complexes as Catalysts for Olefin Epoxidation:  Density Functional Study of Dynamics, <sup>51</sup>V NMR Chemical Shifts, and Mechanism by Michael Bühl (2439988)

    Published 2004
    “…A density functional study of [VO(O<sub>2</sub>)<sub>2</sub>(Im)]<sup>-</sup> (<b>1</b>, Im = imidazole) is presented, calling special attention to effects of dynamics and solvation on the <sup>51</sup>V chemical shift. …”
  2. 15542
  3. 15543

    A New Highly Sensitive Method to Assess Respiration Rates and Kinetics of Natural Planktonic Communities by Use of the Switchable Trace Oxygen Sensor and Reduced Oxygen Concentrati... by Laura Tiano (524349)

    Published 2014
    “…This method provides continuous real time measurements, allowing for a number of diverse possibilities, such as modeling the rate of oxygen decrease to obtain kinetic parameters. …”
  4. 15544
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  6. 15546

    Tunable Electrical Properties of Embossed, Cellulose-Based Paper for Skin-like Sensing by Tongfen Liang (9601461)

    Published 2020
    “…The largest increase in conductivity from 8.38 × 10<sup>–6</sup> to 2.5 × 10<sup>–3</sup> S/m by a factor of ∼300 occurred at a percolation threshold of 3.8 wt % (or 0.36 vol %) with the composite paper plastically compressed by 410 MPa, which caused a decrease of porosity from 88% to 42% on average. …”
  7. 15547

    Tunable Electrical Properties of Embossed, Cellulose-Based Paper for Skin-like Sensing by Tongfen Liang (9601461)

    Published 2020
    “…The largest increase in conductivity from 8.38 × 10<sup>–6</sup> to 2.5 × 10<sup>–3</sup> S/m by a factor of ∼300 occurred at a percolation threshold of 3.8 wt % (or 0.36 vol %) with the composite paper plastically compressed by 410 MPa, which caused a decrease of porosity from 88% to 42% on average. …”
  8. 15548
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  12. 15552

    In combination with <i>Gem3</i><sup><i>BART</i></sup>, Gemin5 knockdown triggers lethality whereas a reduction in the gene copy number of Gemin5 provokes impaired flight. by Rebecca M. Borg (758474)

    Published 2015
    “…In a heterozygous Gemin5 deficient background brought about by a chromosomal deletion (<i>Df(2R)exu1</i><b>)</b>, the hypomorphic <i>Gem3</i><sup><i>BART</i></sup> motor phenotype becomes apparent on the day 5 time point and intensifies with age (middle panel). …”
  13. 15553
  14. 15554

    Synthesis and Reactivity of Heptamethylcyclohexadienyl Rhodium(III) Complexes by Roman A. Pototskiy (8082911)

    Published 2019
    “…Accordingly, the catalytic reaction of 2-phenylpyridine with 3-hexyne in the presence of <b>4</b> (5 mol %) gave the 9,10-diethyl-8a-azaphenanthrene cation in 61% yield. …”
  15. 15555

    Molecular Origin of Photovoltaic Performance in Donor-<i>block</i>-Acceptor All-Conjugated Block Copolymers by Kendall A. Smith (1477033)

    Published 2015
    “…All-conjugated block copolymers may be an effective route to self-assembled photovoltaic devices, but we lack basic information on the relationship between molecular characteristics and photovoltaic performance. Here, we synthesize a library of poly­(3-hexyl­thiophene) (P3HT) <i>block</i> poly­((9,9-dialkyl­fluorene)-2,7-diyl-<i>alt</i>-[4,7-bis­(alkyl­thiophen-5-yl)-2,1,3-benzo­thiadiazole]-2′,2″-diyl) (PFTBT) donor-<i>block</i>-acceptor all-conjugated block copolymers and carry out a comprehensive study of processing conditions, crystallinity, domain sizes, and side-chain structure on photovoltaic device performance. …”
  16. 15556

    Molecular Origin of Photovoltaic Performance in Donor-<i>block</i>-Acceptor All-Conjugated Block Copolymers by Kendall A. Smith (1477033)

    Published 2015
    “…All-conjugated block copolymers may be an effective route to self-assembled photovoltaic devices, but we lack basic information on the relationship between molecular characteristics and photovoltaic performance. Here, we synthesize a library of poly­(3-hexyl­thiophene) (P3HT) <i>block</i> poly­((9,9-dialkyl­fluorene)-2,7-diyl-<i>alt</i>-[4,7-bis­(alkyl­thiophen-5-yl)-2,1,3-benzo­thiadiazole]-2′,2″-diyl) (PFTBT) donor-<i>block</i>-acceptor all-conjugated block copolymers and carry out a comprehensive study of processing conditions, crystallinity, domain sizes, and side-chain structure on photovoltaic device performance. …”
  17. 15557

    Molecular Origin of Photovoltaic Performance in Donor-<i>block</i>-Acceptor All-Conjugated Block Copolymers by Kendall A. Smith (1477033)

    Published 2015
    “…All-conjugated block copolymers may be an effective route to self-assembled photovoltaic devices, but we lack basic information on the relationship between molecular characteristics and photovoltaic performance. Here, we synthesize a library of poly­(3-hexyl­thiophene) (P3HT) <i>block</i> poly­((9,9-dialkyl­fluorene)-2,7-diyl-<i>alt</i>-[4,7-bis­(alkyl­thiophen-5-yl)-2,1,3-benzo­thiadiazole]-2′,2″-diyl) (PFTBT) donor-<i>block</i>-acceptor all-conjugated block copolymers and carry out a comprehensive study of processing conditions, crystallinity, domain sizes, and side-chain structure on photovoltaic device performance. …”
  18. 15558

    Molecular Origin of Photovoltaic Performance in Donor-<i>block</i>-Acceptor All-Conjugated Block Copolymers by Kendall A. Smith (1477033)

    Published 2015
    “…All-conjugated block copolymers may be an effective route to self-assembled photovoltaic devices, but we lack basic information on the relationship between molecular characteristics and photovoltaic performance. Here, we synthesize a library of poly­(3-hexyl­thiophene) (P3HT) <i>block</i> poly­((9,9-dialkyl­fluorene)-2,7-diyl-<i>alt</i>-[4,7-bis­(alkyl­thiophen-5-yl)-2,1,3-benzo­thiadiazole]-2′,2″-diyl) (PFTBT) donor-<i>block</i>-acceptor all-conjugated block copolymers and carry out a comprehensive study of processing conditions, crystallinity, domain sizes, and side-chain structure on photovoltaic device performance. …”
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